Analysis of cytotoxic effects of silver nanoclusters on human peripheral blood mononuclear cells 'in vitro'
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The antimicrobial properties of silver nanoparticles (AgNPs) have made these particles one of the most used nanomaterials in consumer products. Therefore, an understanding of the interactions (unwanted toxicity) between nanoparticles and human cells is of significant interest. The aim of this study was to assess the in vitro cytotoxicity effects of silver nanoclusters (AgNC, < 2nm diameter) on peripheral blood mononuclear cells (PBMC). Using flow cytometry and comet assay methods, we demonstrate that exposure of PBMC to AgNC induced intracellular reactive oxygen species (ROS) generation, DNA damage and apoptosis at 3, 6 and 12h, with a dose-dependent response (0.1, 1, 3, 5 and 30μgml-1). Advanced electron microscopy imaging of complete and ultrathin-sections of PBMC confirmed the cytotoxic effects and cell damage caused by AgNC. The present study showed that AgNC produced without coating agents induced significant cytotoxic effects on PBMC owing to their high aspect ratio and active surface area, even at much lower concentrations (<1μgml-1) than those applied in previous studies, resembling what would occur under real exposure conditions to nanosilver-functionalized consumer products. © 2015 John Wiley %26 Sons, Ltd.
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The antimicrobial properties of silver nanoparticles (AgNPs) have made these particles one of the most used nanomaterials in consumer products. Therefore, an understanding of the interactions (unwanted toxicity) between nanoparticles and human cells is of significant interest. The aim of this study was to assess the in vitro cytotoxicity effects of silver nanoclusters (AgNC, < 2nm diameter) on peripheral blood mononuclear cells (PBMC). Using flow cytometry and comet assay methods, we demonstrate that exposure of PBMC to AgNC induced intracellular reactive oxygen species (ROS) generation, DNA damage and apoptosis at 3, 6 and 12h, with a dose-dependent response (0.1, 1, 3, 5 and 30μgml-1). Advanced electron microscopy imaging of complete and ultrathin-sections of PBMC confirmed the cytotoxic effects and cell damage caused by AgNC. The present study showed that AgNC produced without coating agents induced significant cytotoxic effects on PBMC owing to their high aspect ratio and active surface area, even at much lower concentrations (<1μgml-1) than those applied in previous studies, resembling what would occur under real exposure conditions to nanosilver-functionalized consumer products. © 2015 John Wiley & Sons, Ltd.
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Apoptosis; Comet assay; Cytotoxicity; Nanoparticles; Oxidative stress; PBMC; Silver nanoclusters reactive oxygen metabolite; silver nanoparticle; metal nanoparticle; reactive oxygen metabolite; silver; adult; apoptosis; Article; cell damage; cell membrane; cell viability; cell viability assay; comet assay; controlled study; cytotoxicity; DNA damage; electron microscopy; female; flow cytometry; fluorometry; human; human cell; in vitro study; male; microwave radiation; oxidative stress; peripheral blood mononuclear cell; priority journal; scanning electron microscopy; surface area; cell culture; CFU counting; chemically induced; drug effects; inflammation; metabolism; mononuclear cell; particle size; pathology; surface property; young adult; Adult; Apoptosis; Cells, Cultured; Colony-Forming Units Assay; Comet Assay; DNA Damage; Female; Flow Cytometry; Humans; In Vitro Techniques; Inflammation; Leukocytes, Mononuclear; Male; Metal Nanoparticles; Microscopy, Electron; Particle Size; Reactive Oxygen Species; Silver; Surface Properties; Young Adult
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